Evidence map›Paper›PMID 22389395›Full record

ArticleJournal of cell science2012

Down's-syndrome-related kinase Dyrk1A modulates the p120-catenin-Kaiso trajectory of the Wnt signaling pathway.

Ji Yeon Hong, Jae-Il Park, Moonsup Lee, William A Muñoz, Rachel K Miller, Hong Ji, Dongmin Gu, Jerome Ezan, Sergei Y Sokol, Pierre D McCrea

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Journal of cell science, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
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  9. DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract.Genetics in medicine : official journal of the American College of Medical Genetics · 2019
    Article
  10. Review
  11. Article
  12. Article
  13. The Wnt Signaling Pathway and Related Therapeutic Drugs in Autism Spectrum Disorder.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2018
    Review
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4 · The record

Corrections and comments

  • Erratum issued
    Ezan, Jerome [added]
5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Ji Yeon HongDepartment of Biochemistry and Molecular Biology, University of Texas MD Anderson Cancer Center, Houston, Texas, TX 77030, USA.
Jae-Il Park
Moonsup Lee
William A Muñoz
Rachel K Miller
Hong Ji
Dongmin Gu
Jerome Ezan
Sergei Y Sokol
Pierre D McCrea
The University of Texas MD Anderson Cancer Center · USIcahn School of Medicine at Mount Sinai · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI GIBBONS, DON LYNN · 1996 to 2024
$57.4M
p120-catenin sub-family functionsR01GM052112 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MCCREA, PIERRE D · 1995 to 2010
$3.5M
NCI NIH HHS CA-16672NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA070907NIGMS NIH HHS R01 GM052112NIGMS NIH HHS R01GM52112
6 · The paper itself

Abstract

The Wnt pathways contribute to many processes in cancer and development, with β-catenin being a key canonical component. p120-catenin, which is structurally similar to β-catenin, regulates the expression of certain Wnt target genes, relieving repression conferred by the POZ- and zinc-finger-domain-containing transcription factor Kaiso. We have identified the kinase Dyrk1A as a component of the p120-catenin-Kaiso trajectory of the Wnt pathway. Using rescue and other approaches in Xenopus laevis embryos and mammalian cells, we found that Dyrk1A positively and selectively modulates p120-catenin protein levels, thus having an impact on p120-catenin and Kaiso (and canonical Wnt) gene targets such as siamois and wnt11. The Dyrk1A gene resides within the Down's syndrome critical region, which is amplified in Down's syndrome. A consensus Dyrk phosphorylation site in p120-catenin was identified, with a mutant mimicking phosphorylation exhibiting the predicted enhanced capacity to promote endogenous Wnt-11 and Siamois expression, and gastrulation defects. In summary, we report the biochemical and functional relationship of Dyrk1A with the p120-catenin-Kaiso signaling trajectory, with a linkage to canonical Wnt target genes. Conceivably, this work might also prove relevant to understanding the contribution of Dyrk1A dosage imbalance in Down's syndrome.

Indexed as

Amino Acid SequenceAnimalsBase SequenceCateninsDelta CateninDNA PrimersDown SyndromeGene Expression Regulation, DevelopmentalHEK293 CellsHumansMolecular Sequence DataMutant ProteinsPhosphorylationProtein Serine-Threonine KinasesProtein-Tyrosine KinasesRecombinant ProteinsCateninsDelta CateninDNA PrimersDyrk1A protein, XenopusMutant ProteinsProtein Serine-Threonine KinasesProtein-Tyrosine KinasesRecombinant ProteinsRepressor ProteinsRNA, Small InterferingXenopus ProteinsZBTB33 protein, Xenopus

Identifiers

PMID22389395
PMCPMC3367828
OpenAlexW2097442147

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.